1ODB
THE CRYSTAL STRUCTURE OF HUMAN S100A12 - COPPER COMPLEX
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 120 |
Collection date | 2002-05-15 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 70.569, 118.957, 90.185 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.000 - 2.190 |
R-factor | 0.188 |
Rwork | 0.186 |
R-free | 0.22600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1e8a |
RMSD bond length | 0.014 |
RMSD bond angle | 1.353 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MOLREP |
Refinement software | REFMAC (5.1.24) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 2.270 |
High resolution limit [Å] | 2.190 | 2.190 |
Rmerge | 0.073 | 0.360 |
Number of reflections | 39556 | |
<I/σ(I)> | 18.1 | 3.2 |
Completeness [%] | 99.7 | 97.6 |
Redundancy | 5.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 5-7% PEG 5K MME, 250MM NACL, 5MM CACL2,1MM CUCL2,0.1M NA-CACODYLATE PH 6.5; HANGING-DROP VAPOUR DIFFUSION + SEEDING |